Teleflex Medical recalls Rusch EasyCath Kit
- Recall date
- July 1, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2086-2019
- FDA classification
- Class II
- Brand / firm
- Teleflex Medical
- Sold / distributed
- Nationwide distribution to CA, FL, IL, NC, NJ, OH, OK, TX.
Why it was recalled
Potential for product not to be sterile.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Rusch EasyCath Kit
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